TyTek PneumoDart Decompression Needle
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| NSN | 6515-01-655-9514 |
|---|---|
| Manufacturer | TyTek Medical |
| Model | PneumoDart 14G × 3.25″, Veress safety tip. |
| Kilmės šalis | USA |
| Gaminio tipas | Medical device |
| Features | 14G × 3.25″ (approximately 8.25 cm); Veress safety tip; Luer-lock cap for active removal of air or blood; CoTCCC-recommended dimensions; NSN 6515-01-655-9514. |
| Certificates | FDA cleared; ISO 13485 certified. |
| Sterility | Sterile |
| Expiration date | 3 years. |
| Usage | Needle decompression for tension pneumothorax; management of chest trauma in emergency and tactical medical settings. |
| Warnings | For use by trained professionals only. Needle decompression should only be performed for tension pneumothorax in accordance with the applicable protocol. |
| Storage | Store in a dry place at room temperature in the original packaging. |
| Product dimensions | 14G x 3,25″ (apie 8,25 cm) |
| Spalva | Skaidri |
| Equipment / Configuration | 5 × 5 cm; hydrogel thickness: approximately 3.5 mm. |
TyTek TPAK 14G Decompression Needle
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| NSN | 6515-01-541-0635 |
|---|---|
| Manufacturer | TyTek Medical |
| Model | TPAK 14G x 3,25″Decompression needle. |
| Kilmės šalis | USA |
| Gaminio tipas | Medical device |
| Features | 14G x 3,25″ (8,25 cm); CoTCCC Recommended dimensions; needle-free flash chamber for instant confirmation; |
| Certificates | FDA registration (GUDID), EU Declaration of Conformity (MDR), UDI labeling. |
| Sterility | Sterile |
| Usage | Needle decompression for tension pneumothorax in tactical and military medicine and emergency medical settings. Single-use.. |
| Warnings | For use by trained professionals only. Needle decompression should be performed only in cases of tension pneumothorax and in accordance with the applicable protocol. Immediate medical attention is required following the procedure.. |
| Storage | Store in a dry place at room temperature in the original packaging. |
| Product dimensions | 14G × 3,25″ (8,25 cm) |
| Spalva | Skaidri |
| Equipment / Configuration | 1 × sterile TPAK® TM-303 14G × 3.25” decompression needle with catheter in a protective case.. |
TyTek XTricate Lyte Soft Emergency Stretcher
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| Manufacturer | TyTek Medical |
|---|---|
| Model | XTricate Lyte Soft Emergency Stretcher |
| Kilmės šalis | USA |
| Gaminio tipas | Medical device |
| Features | Lightweight, compact, single-use soft emergency stretcher designed for rapid casualty transport; maximum load tested by an independent laboratory – 226 kg; made from durable polypropylene webbing and lightweight non-woven polypropylene fabric; reinforced polyester stitching; 4 large carrying handles on each side and 2 handles at both the head and foot ends, providing a total of 12 carrying handles. |
| Sterility | Non-sterile. |
| Usage | Rapid casualty transfer and extraction from hazardous areas in tactical, rescue, and industrial situations. |
| Warnings | Inspect the condition of the fabric and carrying handles before use. Casualty transfer should only be performed by trained personnel. |
| Storage | Store folded in a dry place. |
| Equipment / Configuration | 1 × XTricate Lyte TM-512 soft emergency stretcher. |
Vented Chest Seal Kit
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| NSN | 6510-01-642-6212 |
|---|---|
| Manufacturer | North American Rescue, LLC |
| Model | HyFin® Vent Chest Seal Twin Pack |
| Gaminio tipas | Medical device |
| Kilmės šalis | USA |
| Certificates | TCCC ir TECC gairės; EMS Standard of Care; JAV patent 7,504,549 |
| Sterility | Sterile |
| Usage | Use to seal penetrating chest wounds in accordance with the manufacturer’s instructions for use and applicable first aid and emergency medical protocols. Before applying the seal, clean the wound area with the gauze pad included in the kit. Position the transparent seal so that the venting system is correctly aligned over the wound. After application, continuously monitor the patient’s respiratory condition. |
| Equipment / Configuration | 2 × HyFin® Vent Chest Seals + 1 gauze pad for cleaning the wound area with each seal. |
| Warnings | Use the device in accordance with the manufacturer’s instructions for use and applicable medical care protocols. After applying the seal, continuously monitor the patient for any deterioration in respiratory condition and, if necessary, take the measures specified in the applicable protocols. Do not use if the sterile packaging is damaged or if the expiry date indicated on the packaging has passed. For single use only. Do not reuse. |
| Storage | Laikyti originalioje nepažeistoje pakuotėje, laikantis gamintojo pakuotėje ir naudojimo instrukcijoje nurodytų laikymo reikalavimų. Konkrečios laikymo temperatūros ir santykinės drėgmės ribos viešame gamintojo produkto aprašyme nenurodytos. |
Ventiliuojamas krūtinės tvarstis su 360° Hyper-Vent sistema: 24 vožtuvai ir 512 ventiliacijos kanalų.
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| Manufacturer | Celox Medical (MedTrade Products) |
|---|---|
| Model | FoxSeal Vented, 360° Hyper-Vent |
| Kilmės šalis | USA |
| Gaminio tipas | Medical device |
| Features | 360° Hyper-Vent system; 24 valves and 512 ventilation pathways; strong adhesive designed to adhere to wet or hairy skin; suitable for extreme environmental conditions. |
| Certificates | UDI/GTIN; FDA GUDID registration; GMDN. |
| Sterility | Sterile |
| Expiration date | 3 years. |
| Usage | Penetrating chest wounds where continuous evacuation of air from the pleural cavity is required. |
| Product dimensions | 13,0 × 13,3 cm. |
| Warnings | After applying the chest seal, the casualty must be monitored for signs of tension pneumothorax, even when a vented chest seal is used. |
| Storage | Store in a dry place at room temperature in the original packaging. |
| Spalva | Skaidri |
| Equipment / Configuration | 1 × FOXSEAL™ Vented sterile vented chest seal in individual packaging. |
XFLAMM Defender Fire Safety Product
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| Manufacturer | XFlamm GmbH |
|---|---|
| Model | XFLAMM Defender |
| Kilmės šalis | Germany |
| Gaminio tipas | Fire safety measure |
| Certificates | MPA Dresden 43A Fire Class Test Certificate |
| Features | Environmentally friendly, water-based extinguishing agent with active mineral additives. Effectively extinguishes Class A fires, reduces water consumption, leaves no aggressive residues, and is suitable for use with standard water-based firefighting equipment. |
| Usage | Fire protection for facilities and equipment; the exact intended use is subject to confirmation. |
| Warnings | Fire safety products must be used in accordance with the manufacturer’s instructions and applicable regulations. |
| Storage | Store in a dry, easily accessible location. |
XFLAMM Protector Fire Safety Product
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| Manufacturer | XFlamm |
|---|---|
| Model | XFLAMM Protector |
| Kilmės šalis | Germany |
| Gaminio tipas | Fire safety measure |
| Features | Professional flame-retardant impregnation treatment designed to reduce the risk of ignition and the spread of flames in combustible materials. Suitable for wood, textiles, foam, and other absorbent materials, while preserving the natural appearance of the treated surface. Easy to apply by spraying, roller, or brush. |
| Usage | Fire protection for facilities and equipment, the exact intended use is subject to confirmation. |
| Warnings | Fire safety products must be used in accordance with the manufacturer’s instructions and applicable regulations. |
| Storage | Store in a dry, easily accessible location. |
Xtract SR Afloat Flotation Attachment
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| Manufacturer | TSG Associates LLP |
|---|---|
| Model | Xtract SR Afloat |
| Kilmės šalis | United Kingdom |
| Gaminio tipas | Ancillary aid |
| Features | Inflatable, reusable buoyancy module designed for use with Xtract™ SR stretchers; provides 350 N of buoyancy; side and head buoyancy chambers stabilise the casualty and help keep the head above water; features three independently inflatable buoyancy chambers; chambers are inflated through one-way valves; the Xtract SR stretcher is secured to the Afloat module using 11 attachment points; compact and lightweight; designed for casualty evacuation across water obstacles and flooded areas; can also be used as an insulating mattress on land to help reduce heat loss and improve casualty comfort. |
| Certificates | EU MDR 2017/745; UK Medical Devices Regulations 2002 |
| Sterility | Non-sterile |
| Usage | Casualty evacuation in water: maritime, river, and flood rescue operations, as well as military water crossings. |
| Warnings | Inspect the accessory for integrity before use in water. Water rescue operations should only be carried out by trained personnel. |
| Storage | Store in a dry place; after use in water, rinse with fresh water and allow to dry thoroughly. |
| Product dimensions | Unfolded / uninflated dimensions: 2510 × 1010 mm, according to Helix Operations. |
| Spalva | Juoda |
| Equipment / Configuration | 1 × Xtract™ SR Afloat inflatable buoyancy module with integrated buoyancy chambers, attachment points, and inflation valves. |
Xtract SR Base Stretcher Platform
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| NSN | 5340-99-155-7863 |
|---|---|
| Manufacturer | TSG Associates LLP |
| Model | Xtract SR Base |
| Kilmės šalis | United Kingdom |
| Gaminio tipas | Ancillary aid |
| Features | Additional rigidity and abrasion resistance; designed for use with Xtract SR stretchers; NSN 5340-99-155-7863. |
| Sterility | Non-sterile |
| Usage | Stretcher reinforcement and protection when dragging a casualty over rough surfaces and during prolonged evacuations. |
| Warnings | Inspect the condition before use. Do not exceed the load capacity of the stretcher system. |
| Storage | Store in a dry place in the original case. |
| Product dimensions | 2210 × 550 mm (221 × 55 cm) |
| Spalva | Juoda |
| Equipment / Configuration | 1 × Xtract® SR Base rigid drag base + securing straps. |
Xtract SR Casualty Evacuation Stretcher
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| NSN | 6530-99-315-5529 |
|---|---|
| Manufacturer | TSG Associates LLP |
| Model | Xtract SR Stretcher |
| Kilmės šalis | United Kingdom |
| Gaminio tipas | Medical device |
| Features | Weight: approximately 1 kg; load capacity: up to 300 kg; casualty positioning in approximately 30 seconds; Duralite fabric; drawcord and elastic securing system; graphical positioning markings; NSN 6530-99-315-5529. |
| Sterility | Non-sterile |
| Usage | Casualty evacuation from hazardous areas, including dragging, carrying, and transferring during military, rescue, and tactical operations. |
| Warnings | Inspect the condition of the fabric and seams before use. Do not exceed the manufacturer’s specified load capacity. Casualty handling and transfer should only be performed by trained personnel. |
| Storage | Store in a dry place, folded in the original carrying case. |
| Product dimensions | Unfolded stretcher dimensions: approximately 2500 × 900 mm (250 × 90 cm). |
| Spalva | Juoda |
| Equipment / Configuration | 1 × Xtract™ SR Stretcher textile evacuation stretcher. |
Z-Medica Hemorrhage Control Training Kit
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| NSN | 6910-01-642-7321 |
|---|---|
| Manufacturer | Teleflex (Z-Medica) |
| Model | Hemorrhage Control Training Kit |
| Kilmės šalis | USA |
| Gaminio tipas | Teaching aid |
| Features | Professional bleeding control training kit with a realistic training limb and QuikClot® Combat Gauze training products. Designed for hands-on training in wound packing, tourniquet application, and life-threatening bleeding control in accordance with TCCC, TECC, and Stop the Bleed® training programs. |
| Certificates | DAPA |
| Warnings | FOR TRAINING USE ONLY. Not intended for use on patients or actual wounds. Store separately from medical devices intended for clinical use to prevent accidental mix-ups. |
| Storage | Store in a dry place at room temperature, separately from medical devices intended for clinical use; protect from direct sunlight. |
| Equipment / Configuration | 1 × training leg with simulated wounds; 5 × QuikClot Combat Gauze Moulage Trainers; 5 × QuikClot Combat Gauze hemostatic dressings; 2 × QuikClot Combat Gauze XL hemostatic dressings. |